Awindra pandey biography of williams syndrome

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Williams syndrome (WS) is a multi-system disorder caused by a microdeletion on chromosome 7q.

NCBI Bookshelf. Marcia Wilson ; Iverson B. Authors Marcia Wilson ; Iverson B. Carter 1. Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features elfin-like faces , hypercalcemia, neurodevelopmental, and behavioral deficits. This activity reviews the diagnostic evaluation, treatment, and interprofessional management of Williams syndrome and highlights the role of the interprofessional team in evaluating and treating patients with this condition.

Williams syndrome (WS) is a rare genetic disorder characterized by heart disease, failure to thrive, hearing loss, intellectual or learning disability, speech and language delay, Missing: awindra pandey.

Objectives: Identify the etiology and epidemiology of Williams syndrome. Describe the appropriate history, physical examination, and evaluation for patients with Williams syndrome. Summarize the management strategies and treatment options available for patients with Williams syndrome. Outline strategies that interprofessional teams may use to improve management and outcomes in patients with Williams syndrome.

Access free multiple choice questions on this topic. Williams syndrome WS is a rare genetic and neurodevelopmental disorder. WS often presents at birth when the child is discovered to have supra-vascular aortic stenosis. Cardiologist Dr.